Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11736859
rs11736859
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105787628 intron variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17036225
rs17036225
INTS12 ; GSTCD ; GSTCD-AS1 ; LOC107986190
2 4 105788935 intron variant A/G;T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs17036230
rs17036230
INTS12 ; GSTCD ; GSTCD-AS1 ; LOC107986190
2 4 105793991 intron variant T/A snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11727745
rs11727745
INTS12 ; GSTCD ; GSTCD-AS1 ; LOC107986190
2 4 105795370 intron variant T/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11097901
rs11097901
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105808776 intron variant C/T snv 5.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs10516527
rs10516527
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105813189 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs10516528
rs10516528
INTS12 ; GSTCD ; GSTCD-AS1
3 4 105818436 intron variant G/T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11731417
rs11731417
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824855 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11723225
rs11723225
INTS12 ; GSTCD ; GSTCD-AS1
2 4 105824908 intron variant C/T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11732650
rs11732650
INTS12 ; GSTCD
2 4 105833074 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs11728716
rs11728716
INTS12 ; GSTCD
2 4 105834839 intron variant G/A snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs7676975
rs7676975
INTS12 ; GSTCD
2 4 105842654 intron variant A/T snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs11733223
rs11733223
INTS12 ; GSTCD
2 4 105844368 intron variant C/A snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs10050333
rs10050333
INTS12 ; GSTCD
2 4 105844656 intron variant T/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs10050159
rs10050159
INTS12 ; GSTCD
2 4 105844758 intron variant G/A snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs11722225
rs11722225
INTS12 ; GSTCD
5 4 105845273 intron variant T/C snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs11726124
rs11726124
INTS12 ; GSTCD
2 4 105845339 intron variant A/G snv 5.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs7660534
rs7660534
INTS12
2 4 105874890 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17036341
rs17036341
INTS12
2 4 105875672 intron variant C/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs10516529
rs10516529
INTS12
2 4 105878159 intron variant T/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs11730660
rs11730660
INTS12
2 4 105879222 intron variant A/C snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs17331332
rs17331332
INTS12
4 4 105886950 intron variant G/A snv 4.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs2798641
rs2798641
ARMC2
5 6 108946847 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs11067283
rs11067283
LOC107984437
2 12 114758086 intron variant T/A snv 0.24 0.700 1.000 1 2010 2010
dbSNP: rs11598305
rs11598305
CDC123
2 10 12227401 intron variant C/A;G snv 0.700 1.000 1 2010 2010